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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1881668Generated: November 2, 2026

5-Aminoindole → HCID 15521320, compound

https://huagongshe.com/reaction/1881668

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-AminoindoleHCID 78867—
Reactant4-Chloro-6-iodoquinazolineHCID 11173809—
ProductHCID 15521320HCID 15521320—

Reaction Steps

JP-A-10-152477 describes a process for preparing a 4-arylaminoquinazoline compound from a quinazolin-4-one, which comprises the steps of chlorinating 4-iodoquinazolin-4-one using an excessive amount of oxalyl chloride to produce 6-iodo-4-chloroquinazoline (intermediate compound), concentrating the reaction product under reducing pressure to isolate the resulting product; reacting the 6-iodo-4-chloroquinazoline with 5-aminoindole to give 6-iodo-4 (5-indolylamino)quinazoline. Unfortunately, the yield is not high. Further, it should be noted that the intermediate compound, i.e., 4-chloroquinazoline compound, shows no satisfactory stability in the presence of water and no satisfactory resistance to heat. Accordingly, the compound should be handled carefully.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08318932B2
Source datasetuspto-grants-2012_11
ORD IDord-8af571ed92d9496799f655e9d5732b86
Source noteuspto-grants-2012_11